A kind of preparation method of rosuvastatin sodium

A technology for rosuvastatin sodium and substance, applied in the field of preparation of rosuvastatin sodium, can solve the problems of high route cost, poor atom economy, difficult to obtain side chains and the like

Active Publication Date: 2022-05-27
ANHUI QINGYUN PHARMA & CHEM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0019] Although the stereoselectivity of docking in this route has been well resolved, the side chains are difficult to obtain, the atom economy of the reaction is poor, and the olefination reaction temperature is -60°C, which requires high equipment, which makes the industrial production of this route difficult.
[0020] From the above review, it can be seen that the current synthesis of rosuvastatin sodium is difficult to obtain because of expensive raw materials, or because the route is complex and the total yield is low, or because the reaction conditions are harsh, it is difficult to realize industrial production, or because of the poor stereoselectivity, the cost of the route is high. , so the development of cheap and easy-to-obtain raw materials, mild reaction conditions, and good atom economy has broad prospects

Method used

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  • A kind of preparation method of rosuvastatin sodium
  • A kind of preparation method of rosuvastatin sodium
  • A kind of preparation method of rosuvastatin sodium

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0076] A preparation method of rosuvastatin sodium, comprising the steps of: (4R-Cis)-6-hydroxymethyl-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester Carry out sulfonylation reaction with p-toluenesulfonyl chloride under the action of catalyst to obtain (4R-Cis)-6-p-toluenesulfonyl-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester; then react with trimercapto-s-triazine under the action of a basic catalyst to obtain substance A; then oxidize to obtain substance B through the action of an oxidant; and then react with 4-(4-fluorophenyl)-6-isopropyl-2-[ (N-methyl-N-methylsulfonyl)amino]pyrimidine-5-carbaldehyde reacted under the catalysis of sodium hydride to obtain substance C; finally deprotected by hydrochloric acid, hydrolyzed into a salt by sodium hydroxide to obtain rosuvastatin sodium.

Embodiment 2

[0078] A preparation method of rosuvastatin sodium, comprising the steps of:

[0079] Mix (4R-Cis)-6-hydroxymethyl-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester, dimethylamine, dichloromethane and cool down to - 5°C, dropwise add the dichloromethane solution of p-toluenesulfonyl chloride, during the dropwise addition, keep the temperature not exceeding 5°C, reflux for 24 hours after the dropwise addition, wash with water, extract the organic phase with dichloromethane, dry, and concentrate to obtain (4R -Cis)-6-p-toluenesulfonyl-2,2-dimethyl-1,3-dioxane-4-tert-butyl acetate, wherein (4R-Cis)-6-hydroxymethyl-2 , The molar ratio of 2-dimethyl-1,3-dioxane-4-tert-butyl acetate to dimethylamine is 1:1.5, (4R-Cis)-6-hydroxymethyl-2,2- The molar ratio of dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester to p-toluenesulfonyl chloride is 1:1.5;

[0080] In a nitrogen atmosphere, trimercapto-s-triazine, sodium hydroxide, 1,4-dioxane, (4R-Cis)-6-p-toluenesulfonyl-2,2-dimeth...

Embodiment 3

[0085] A preparation method of rosuvastatin sodium, comprising the steps of:

[0086] Mix (4R-Cis)-6-hydroxymethyl-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester, pyridine and dichloromethane, cool to -2°C , dropwise add a dichloromethane solution of p-toluenesulfonyl chloride, keep the temperature not exceeding 5°C during the dropwise addition, reflux for 18h after the dropwise addition, wash with water, extract the organic phase with dichloromethane, dry, and concentrate to obtain (4R-Cis )-6-p-toluenesulfonyl-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester, wherein, (4R-Cis)-6-hydroxymethyl-2,2 -Dimethyl-1,3-dioxane-4-tert-butyl acetate to pyridine in a molar ratio of 1:2, (4R-Cis)-6-hydroxymethyl-2,2-dimethyl- The molar ratio of 1,3-dioxane-4-acetic acid tert-butyl ester to p-toluenesulfonyl chloride is 1:1.3;

[0087] In a nitrogen atmosphere, trimercapto-s-triazine, potassium hydroxide, 1,4-dioxane, (4R-Cis)-6-p-toluenesulfonyl-2,2-dimethyl-1,3- Mix t...

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Abstract

The invention discloses a preparation method of rosuvastatin sodium, comprising the following steps: (4R-Cis)-6-hydroxymethyl-2,2-dimethyl-1,3-dioxane-4- The sulfonylation reaction of tert-butyl acetate and p-toluenesulfonyl chloride under the action of a catalyst gives (4R-Cis)-6-p-toluenesulfonyl-2,2-dimethyl-1,3-dioxane-4 ‑tert-butyl acetate; then react with trimercapto-s-triazine under the action of a basic catalyst to obtain substance A; then oxidize with oxidant to obtain substance B; then react with 4‑(4‑fluorophenyl)‑6‑isopropyl ‑2‑[(N‑Methyl‑N‑methylsulfonyl)amino]pyrimidine‑5‑formaldehyde is reacted under the catalysis of sodium hydride to obtain substance C; finally deprotected by hydrochloric acid, and sodium hydroxide is hydrolyzed into a salt to obtain rosuvastatin sodium.

Description

technical field [0001] The invention relates to the technical field of chemical substance preparation, in particular to a preparation method of rosuvastatin sodium. Background technique [0002] Rosuvastatin Calcium is an anti-hyperlipidemic drug, which is an HMG-CoA reductase inhibitor, successfully developed by British AstraZeneca, and is suitable for the treatment of various lipid abnormalities, including hypercholesterolemia, mixed lipid Massive disorders and simple hypertriglyceridemia. Rosuvastatin calcium is the statin drug with the strongest lipid-lowering effect and the most comprehensive lipid-lowering effect among the blood-lipid-lowering drugs currently on the market. It has better lowering of LDL cholesterol and Improve the effect of high-density lipoprotein, and have better tolerance, lower side effects and unique pharmacokinetic characteristics, rosuvastatin sodium is the precursor of rosuvastatin calcium, therefore, study rosuvastatin The synthetic route of...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07D239/42C07D319/06C07D405/14C07D405/06
CPCC07D239/42C07D319/06C07D405/06C07D405/14C07B2200/07Y02P20/55
Inventor 黄欢黄庆云李凯张宏远
Owner ANHUI QINGYUN PHARMA & CHEM
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